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Author/Creator Koenig, Rainer

1. Deletions in the 3′ Part of the NFIX Gene Including a Recurrent Alu‐Mediated Deletion of Exon 6 and 7 Account for Previously Unexplained Cases of Marshall–Smith Syndrome. Issue 9 (8th July 2014)

Authors:
Schanze, Denny; Neubauer, Dorothée; Cormier‐Daire, Valerie; Delrue, Marie‐Ange; Dieux‐Coeslier, Anne; Hasegawa, Tomonobu; Holmberg, Eva E.; Koenig, Rainer; Krueger, Gabriele; Schanze, Ina; Seemanova, Eva; Shaw, Adam C.; Vogt, Julie; Volleth, Marianne; Reis, André; Meinecke, Peter; Hennekam, Raoul...
Journal:
Human mutation
Issue:
Volume 35:Issue 9(2014:Sep.)
Page Start:
1092
Record Type:
Journal Article
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3. Expansion of the genotypic and phenotypic spectrum in patients with KRAS germline mutations. Issue 2 (20th October 2006)

Authors:
Zenker, Martin; Lehmann, Katarina; Schulz, Anna Leana; Barth, Helmut; Hansmann, Dagmar; Koenig, Rainer; Korinthenberg, Rudolf; Kreiss-Nachtsheim, Martina; Meinecke, Peter; Morlot, Susanne; Mundlos, Stefan; Quante, Anne S; Raskin, Salmo; Schnabel, Dirk; Wehner, Lars-Erik; Kratz, Christian P; Horn,...
Journal:
Journal of medical genetics
Issue:
Volume 44:Issue 2(2007)
Page Start:
131
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗